Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.
- NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_assertion description "[Genetic analysis for PHEO/paraganglioma genes (SDH A-D, SDHAF2, RET, VHL, TMEM127, and MAX), and pituitary-related genes (AIP, MEN1, and p27) were negative.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.
- NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_assertion evidence source_evidence_literature NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.
- NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_assertion SIO_000772 23295290 NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.
- NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_assertion wasDerivedFrom befree-20140225 NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.
- NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_assertion wasGeneratedBy ECO_0000203 NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP681222.RAqSjKheLBtm8qfo3gEGRikyIfLbB93IRM4x267b6NXrs130_provenance.